NCT06988709

Brief Summary

The purpose of our study is to establish the most effective running retraining technique to decrease ground contact time. This will be investigated by applying three running retraining conditions and assessing the change in ground contact time and other biomechanical variables between the runner's baseline running and each retraining technique.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
7mo left

Started May 2025

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress64%
May 2025Dec 2026

First Submitted

Initial submission to the registry

April 18, 2025

Completed
13 days until next milestone

Study Start

First participant enrolled

May 1, 2025

Completed
24 days until next milestone

First Posted

Study publicly available on registry

May 25, 2025

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

December 12, 2025

Status Verified

December 1, 2025

Enrollment Period

1.6 years

First QC Date

April 18, 2025

Last Update Submit

December 5, 2025

Conditions

Keywords

runninggroundgaitretrainingcontacttime

Outcome Measures

Primary Outcomes (1)

  • Ground Contact Time

    The amount of time in milliseconds that the foot remains in contact with the ground while running. GCT will be measured through the RunScribe device.

    Within a single session, measured pre-intervention (baseline) and during each running condition intervention

Secondary Outcomes (4)

  • Step Rate

    Within a single session, measured pre-intervention (baseline) and during each running condition intervention

  • Average Vertical Loading Rate (AVLR)

    Within a single session, measured pre-intervention (baseline) and during each running condition intervention

  • Braking Impulse

    Within a single session, measured pre-intervention (baseline) and during each running condition intervention

  • Step Length

    Within a single session, measured pre-intervention (baseline) and during each running condition intervention

Study Arms (1)

Run Retraining Conditions

EXPERIMENTAL

Single-arm, within subject, repeated measures design. All participants will run at baseline and then under 3 different running conditions.

Other: Real-time Visual FeedbackOther: Real-time Auditory FeedbackOther: Real-time Verbal Feedback

Interventions

Runners will be instructed to match their step rate to a target step rate, 10% above their baseline step rate. A metronome will be played over a speaker to provide real-time auditory feedback of the target step rate.

Run Retraining Conditions

The clinician will provide real-time verbal feedback to runner to "pull your foot off the ground as quickly as you can," every 15 seconds during the retraining condition.

Run Retraining Conditions

Runners will visualize their real-time ground contact time (GCT) measured by the RunScribe on a TV screen. They will be instructed to run with a goal of matching their target GCT. Their target GCT will be 5% less than their baseline.

Run Retraining Conditions

Eligibility Criteria

Age17 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Military Service Member or USMA cadet between the ages of 17-60
  • Run at least 2 miles three times per week for the past 3 months
  • Able to run for at least 15 continuous minutes at a self-selected speed
  • Fluent in the English language to read and provide informed consent and follow study instructions

You may not qualify if:

  • Lower extremity or low back pain in the previous 3 months
  • Lower extremity or low back surgery in the previous 6 months
  • Self-reported pregnancy or given birth within the last 6 months
  • Currently on a profile that restricts or limits running

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Keller Army Community Hospital

West Point, New York, 10996, United States

RECRUITING

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Model Details: Within-subjects, repeated measures design completed in a single session
Sponsor Type
FED
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

April 18, 2025

First Posted

May 25, 2025

Study Start

May 1, 2025

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

December 12, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

We do not have a data sharing agreement or plan to share IDP as part of our IRB protocol.

Locations